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Published June 4, 2026 | Version v2
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Synthesis of Self

Description

This paper formalizes the Synthesis of Self, an information-theoretic framework integrating the Free Energy Principle and functional hemispheric lateralization into a unified computational neuroscience architecture. We model the brain as an asymmetrical dual-processor system, quantifying the dynamics between a discrete tokenization engine (the language-dominant "Manager" network) and a continuous, analog field-processor (the relational "Architect" network"). Crucially, the framework formalizes the longitudinal ontogeny of the self, providing a rigorous computational account of how human identity architecture constructs, scales, and stabilizes over developmental time. By evaluating the transcallosal Coupling Coefficient (C), the model maps how early relational inputs program the system's baseline network and how subsequent fractional variations dictate macro-structural integration. A mathematical degradation in the C metric forces a predictable operational shift: the language-dominant processor uncouples from the relational network's macro-trajectory, downshifting into high-frequency, closed-loop processing that traps the system in automated behavioral loops.

Demonstrating profound abductive consilience, this architecture systematically retrodicts the neurobiological topologies of six major clinical phenotypes—Schizophrenia, Anorexia Nervosa, Bipolar Disorder, Borderline Personality Disorder, Pathological Narcissism, and Obsessive-Compulsive Disorder—while resolving long-standing anomalies in early developmental lateralization. By anchoring the dynamic spectrum of C within triangulated biophysical layers—resting-state Voxel-Mirrored Homotopic Connectivity (VMHC), Dynamic Causal Modeling (DCM), and paired-pulse Transcranial Magnetic Stimulation (TMS)—this framework replaces descriptive syndromic classification with an objective, coordinate-based quantization of network processing failures. This introduces a scalable, responsive biophysical metric to measure cross-hemispheric integration, providing modern neuroscience with the definitive cartography to track systemic decay and precision-target mechanism-specific, non-linear neurostimulation and therapeutic interventions.

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